Junel Fe 1.5/30
Product Images NDC 42254-242

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Junel Fe 1.5/30 (NDC 42254-242). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Rebel Distributors Corp, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Norethindrone Acetate Structural Formula (Eaf4191c 5b2f 47bd B315 F695f8773260 01)

Chemical structure of Norethindrone Acetate, visible as a detailed molecular diagram depicting the steroid backbone with labeled functional groups.*

FDA Label Image

Ethinyl Estradiol Structural Formula (Eaf4191c 5b2f 47bd B315 F695f8773260 02)

Chemical structure of Ethinyl Estradiol. The diagram shows the molecular framework with labeled functional groups typical of the active ingredient Ethinyl Estradiol.*

FDA Label Image

Table Ii (Eaf4191c 5b2f 47bd B315 F695f8773260 03)

A bar chart showing mortality rate (number of deaths per 100,000 women) across different age groups (15-24, 25-34, 35-44, 45+) segmented by smoking status (ever-users, controls) with separate data for smokers and non-smokers.*

FDA Label Image

Junel Fe 1.5/30mcg (Eaf4191c 5b2f 47bd B315 F695f8773260 04)

Junel Fe 1.5/30mcg 28-Day Regimen tablets label showing the product name, strength, dosage form as 1X28 tablets. Labeler is Rebel Distributors Corp, manufactured by Teva Pharmaceuticals USA in Sellersville, PA. Includes storage instructions to keep at controlled room temperature between 15-30°C (59-86°F) and to keep out of reach of children. The label also identifies the product ID SJ024228 and NDC 42254-242-28.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.